Ultracryotomy of biological tissues to preserve membrane structure

1976 ◽  
Vol 20 (3) ◽  
pp. 687-698
Author(s):  
S. Hodson ◽  
L. Williams

A vacuum transfer stage is described which permits visualization of ultracryotome sections without the considerable distortions found in sections which have either thawed or rehydrated after freeze drying. Membrane structure-nucleus, nucleolus, mitochondria with their cristae and plasma membrane-was observed only in cells at the surface of the tissue which had undergone the fastest freezing rates. Inspection of knife damage in sections through these superficial cells showed that glass or diamond knives which are perfectly adequate for sectioning resin-embedded tissues are less suited to sectioning frozen biological tissue. Deeper in the tissue, where the freezing rates were slower, ice crystal cavities destroyed all membranous structures.

Author(s):  
Fang Zhao ◽  
Zhenqian Chen

Biological tissues undergo complex phase change heat transfer processes during cryosurgery, and a theoretical model is preferable to forecast this heat experience. A mathematical model for phase change heat transfer in cryosurgery was established. In this model, a fractal treelike branched network was used to describe the complicated geometrical frame of blood vessels. The temperature distribution and ice crystal growth process in biological tissue including normal tissue and tumor embedded with two cryoprobes were numerically simulated. The effects of cooling rate, initial temperature, and distance of two cryoprobes on freezing process of tissue were also studied. The results show that the ice crystal grows more rapidly in the initial freezing stage (<600 s) and then slows down in the following process, and the precooling of cryoprobes has no obvious effect on freezing rate of tissue. It also can be seen that the distance of 10 mm between two cryoprobes produces an optimal freezing effect for the tumor size (20 mm × 10 mm) in the present study compared with the distances of 6 mm and 14 mm. The numerical results are significant in providing technical reference for application of cryosurgery in clinical medicine.


1971 ◽  
Vol 49 (12) ◽  
pp. 2075-2079 ◽  
Author(s):  
J. A. Brushaber ◽  
S. F. Jenkins Jr.

A study of the vesicular and tubular bodies observed in cells of Poria monticola was done with particular regard to their form, origin, and membrane structure. The membranes of lomasomes and pinocytotic vesicles display the sometimes asymmetric, distinctly trilaminar structure characteristic of the plasma membrane. Lomasomes are abundant and vary in appearance depending upon the method of fixation used. Nonlamellar associations of vesicles and short tubules probably represent the true structure of lomasomes in this organism. These lomasomes originate from the plasma membrane and do not appear to be associated exclusively with wall formation.


Author(s):  
H. K. Plummer ◽  
E. Eichen ◽  
C. D. Melvin

Much of the work reported in the literature on cellulose acetate reverse osmosis membranes has raised new and important questions with regard to the dense or “active” layer of these membranes. Several thickness values and structures have been attributed to the dense layer. To ensure the correct interpretation of the cellulose acetate structure thirteen different preparative techniques have been used in this investigation. These thirteen methods included various combinations of water substitution, freeze drying, freeze sectioning, fracturing, embedding, and microtomy techniques with both transmission and scanning electron microscope observations.It was observed that several factors can cause a distortion of the structure during sample preparation. The most obvious problem of water removal can cause swelling, shrinking, and folds. Improper removal of embedding materials, when used, can cause a loss of electron image contrast and, or structure which could hinder interpretation.


1998 ◽  
Vol 30 (4-5) ◽  
pp. 328-329 ◽  
Author(s):  
V. K. Rybal'chenko

Science ◽  
1977 ◽  
Vol 196 (4293) ◽  
pp. 1005-1007 ◽  
Author(s):  
D. Schotland ◽  
E Bonilla ◽  
M Van Meter

1979 ◽  
Vol 39 (1) ◽  
pp. 355-372
Author(s):  
N.J. Lane ◽  
J.B. Harrison

The occurrence of an unusual double plasma membrane structure is reported; it has been studied in conventional thin sections, after lanthanum-impregnation and with freeze-fracturing. This modification of the plasmalemma is found where the luminal cell membrane (I membrane) of gut microvilli in the haematophagous insect, Rhodnius prolixus, is surrounded by a second, outer membrane (O membrane), the 2 separated from one another by a highly regular I-O space of about 10 nm. Lanthanum impregnation reveals the presence of columns inclined at an angle, within this I-O space; as in the continuous junctions which link the lateral borders of these cells, these columns may maintain the very precise I-O distance. From the outer microvillar membranes radiate short spoke-like fibrils or sheets which encounter another more extensive system of myelin-like sheets. Freeze-fracturing reveals that the spoke-like sheets and the other ones which lie like a tube, around and parallel to the microvilli, contain linear ridges composed of particles, lying at random within layers of the myelin-like material which also extends into the lumen of the gut. The microvillar membanes, both O and I, fracture into faces containing rows of either PF particles or EF pits arranged as spiral ridges or grooves around the sides and across the tip of each microbillus. These could be the insertion sites of one or both of the I-O columns and spoke-like sheets while the sheets could represent a variant of peritrophic membrane. The double membrane may be a cellular device to increase the strength of the microvillar layer in these blood-sucking animals, since the cell layer must withstand great pressure owing to a sudden massive extension of the gut during a blood meal.


2015 ◽  
Vol 77 (28) ◽  
Author(s):  
Azmi Abou Basaif ◽  
Nashrul Fazli Mohd Nasir ◽  
Zulkarnay Zakaria ◽  
Ibrahim Balkhis ◽  
Shazwani Sarkawi ◽  
...  

The enhanced ability to detect accurate location and measure the depth of a   metal inside a biological tissue is very useful in the assessment of medical condition and treatment. This manuscript proposed a solution via the measurement of the tissue properties using magnetic induction spectroscopy (MIS) method to describe the characterization of biological soft tissue. The objective of this study is to explore the viability of locating embedded metal inside a biological tissue by measuring the differences the biological tissue electrical properties using principle of Magnetic Induction Spectroscopy (MIS). Simulation is done using COMSOL Multiphysics software for accurate information on the involved parameters for both metal and biological tissues. Simulation has confirmed that MIS capable of detecting and locate embedded metal inside a biological tissue.


1994 ◽  
Vol 309 (2) ◽  
pp. 369-376 ◽  
Author(s):  
F. Schroeder ◽  
S.M. Colles ◽  
G.P. Kreishman ◽  
C.E. Heyliger ◽  
W.G. Wood

2017 ◽  
Vol 19 (5) ◽  
pp. 1377-1386 ◽  
Author(s):  
Vineet Kumar ◽  
Tot Bui Nguyen ◽  
Beáta Tóth ◽  
Viktoria Juhasz ◽  
Jashvant D. Unadkat

Sign in / Sign up

Export Citation Format

Share Document